Canonical Allele Identifier: CA2540305689

Gene: CYP2C19

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94852474_94852475insCAATGCTTTCCGAGTCCAAGGATCATTCCCTGACCATGACCGAGCTGGCAATCACTACGAACACTCTTCCCGCACGCCTCTCACGAGTCGTAGCGCGTTTGGAGAAGGATGGATACGTCCGCCGTTCCCTC , CM000672.2:g.94852474_94852475insCAATGCTTTCCGAGTCCAAGGATCATTCCCTGACCATGACCGAGCTGGCAATCACTACGAACACTCTTCCCGCACGCCTCTCACGAGTCGTAGCGCGTTTGGAGAAGGATGGATACGTCCGCCGTTCCCTC	GRCh38
NC_000010.10:g.96612231_96612232insCAATGCTTTCCGAGTCCAAGGATCATTCCCTGACCATGACCGAGCTGGCAATCACTACGAACACTCTTCCCGCACGCCTCTCACGAGTCGTAGCGCGTTTGGAGAAGGATGGATACGTCCGCCGTTCCCTC , CM000672.1:g.96612231_96612232insCAATGCTTTCCGAGTCCAAGGATCATTCCCTGACCATGACCGAGCTGGCAATCACTACGAACACTCTTCCCGCACGCCTCTCACGAGTCGTAGCGCGTTTGGAGAAGGATGGATACGTCCGCCGTTCCCTC	GRCh37
NC_000010.9:g.96602221_96602222insCAATGCTTTCCGAGTCCAAGGATCATTCCCTGACCATGACCGAGCTGGCAATCACTACGAACACTCTTCCCGCACGCCTCTCACGAGTCGTAGCGCGTTTGGAGAAGGATGGATACGTCCGCCGTTCCCTC	NCBI36
NG_008384.2:g.94769_94770insCAATGCTTTCCGAGTCCAAGGATCATTCCCTGACCATGACCGAGCTGGCAATCACTACGAACACTCTTCCCGCACGCCTCTCACGAGTCGTAGCGCGTTTGGAGAAGGATGGATACGTCCGCCGTTCCCTC
NG_008384.3:g.94794_94795insCAATGCTTTCCGAGTCCAAGGATCATTCCCTGACCATGACCGAGCTGGCAATCACTACGAACACTCTTCCCGCACGCCTCTCACGAGTCGTAGCGCGTTTGGAGAAGGATGGATACGTCCGCCGTTCCCTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371321.9:c.1292-259_1292-258insCAATGCTTTCCGAGTCCAAGGATCATTCCCTGACCATGACCGAGCTGGCAATCACTACGAACACTCTTCCCGCACGCCTCTCACGAGTCGTAGCGCGTTTGGAGAAGGATGGATACGTCCGCCGTTCCCTC MANE Select	ENSP00000360372.3:n.1292-259_1292-258insCAATGCTTTCCGAGTCCAAGG...
ENST00000645461.1:n.2203-259_2203-258insCAATGCTTTCCGAGTCCAAGGATCATTCCCTGACCATGACCGAGCTGGCAATCACTACGAACACTCTTCCCGCACGCCTCTCACGAGTCGTAGCGCGTTTGGAGAAGGATGGATACGTCCGCCGTTCCCTC
ENST00000371321.7:c.1292-259_1292-258insCAATGCTTTCCGAGTCCAAGGATCATTCCCTGACCATGACCGAGCTGGCAATCACTACGAACACTCTTCCCGCACGCCTCTCACGAGTCGTAGCGCGTTTGGAGAAGGATGGATACGTCCGCCGTTCCCTC	ENSP00000360372.3:n.1292-259_1292-258insCAATGCTTTCCGAGTCCAAGG...
ENST00000464755.1:c.2055-259_2055-258insCAATGCTTTCCGAGTCCAAGGATCATTCCCTGACCATGACCGAGCTGGCAATCACTACGAACACTCTTCCCGCACGCCTCTCACGAGTCGTAGCGCGTTTGGAGAAGGATGGATACGTCCGCCGTTCCCTC	ENSP00000483243.1:n.2055-259_2055-258insCAATGCTTTCCGAGTCCAAGG...
NM_000769.2:c.1292-259_1292-258insCAATGCTTTCCGAGTCCAAGGATCATTCCCTGACCATGACCGAGCTGGCAATCACTACGAACACTCTTCCCGCACGCCTCTCACGAGTCGTAGCGCGTTTGGAGAAGGATGGATACGTCCGCCGTTCCCTC	NP_000760.1:n.1292-259_1292-258insCAATGCTTTCCGAGTCCAAGGATCATT...
NM_000769.4:c.1292-259_1292-258insCAATGCTTTCCGAGTCCAAGGATCATTCCCTGACCATGACCGAGCTGGCAATCACTACGAACACTCTTCCCGCACGCCTCTCACGAGTCGTAGCGCGTTTGGAGAAGGATGGATACGTCCGCCGTTCCCTC MANE Select	NP_000760.1:n.1292-259_1292-258insCAATGCTTTCCGAGTCCAAGGATCATT...